bioRxiv

DNA marks in King penguin blood may record stem-cell aging

An observational analysis of 126 whole-blood DNA profiles identified 409 genes with age-linked changes in chemical marks throughout life.

Fig. 1. Time-associated signals are prevalent throughout the King penguin methylome.
Open the figure at full size
Fig. 1. Time-associated signals are prevalent throughout the King penguin methylome.Time-associated signals are prevalent throughout the King penguin methylome.Hukkanen et al., CC BY-NC-ND
Preprint: experiments in animalsBiomarkers
Follow

In an observational study of King penguins of known ages, researchers analysed 126 whole-blood profiles of DNA methylation, chemical marks on DNA. Red blood cells containing DNA dominate penguin blood, limiting the influence of differences in white blood cell types.

The researchers identified 409 genes whose methylation changed with age throughout life. This set was rich in genes regulating blood-forming stem and precursor cells, which produce blood cells, and communication with their surroundings. Many of the strongest age signals involved genes inactive in mature red blood cells, consistent with marks persisting from earlier blood-forming cells. Comparison with DNA methylation profiles from 1,501 humans found some shared aging-linked genes. An age model using only human counterparts of penguin aging genes predicted people’s ages with high accuracy and remained largely insensitive to the mix of blood cell types.

Why it matters

The work addresses whether age-linked DNA marks in blood reflect cellular aging programmes or changes in the mix of cells—a distinction important for interpreting blood-based aging signatures.

Caveats

The observational data do not establish that the age-linked marks came from earlier blood-forming cells. The paper is a preprint and has not yet been peer-reviewed.

From the paper

Participants

To systematically evaluate this, we conducted an epigenome-wide association study (EWAS) using Illumina 450K BeadChip data from 1,501 human twins across 761 families (Supplementary Table 2).

Results, Conserved epigenetic aging signatures in King penguins and humans

Result

We found that genes with an open promoter were much more likely to be expressed than genes with a closed promoter (Fisher’s exact test: odds ratio = 27.3, 95% CI 25.0-29.9, p-value < 2.2e⁻¹⁶; n = 18,140 genes).

Results, Core HSPC-linked aDMGs are not active in blood

Limitation

An important limitation of our study is that our data was restricted to peripheral blood DNA methylation without paired multi-omic or clinical health indices.

Limitations of this study

Quoted word for word from the full text on bioRxiv.